Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?

Gelijkaardige items

• The phenotypic spectrum of X‐linked, infantile onset ALG13‐related developmental and epileptic encephalopathy
  door: Datta, Alexandre N., et al.
  Gepubliceerd in: (2021)
• Electroclinical Features of Early-Onset Epileptic Encephalopathies in Congenital Disorders of Glycosylation (CDGs)
  door: Fiumara, Agata, et al.
  Gepubliceerd in: (2015)
• Pubertal development in ALG6 deficiency (congenital disorder of glycosylation type Ic)
  door: Miller, Bradley S., et al.
  Gepubliceerd in: (2011)
• SCN1B‐linked early infantile developmental and epileptic encephalopathy
  door: Aeby, Alec, et al.
  Gepubliceerd in: (2019)
• Epidemiology and etiology of infantile developmental and epileptic encephalopathies in Tasmania
  door: Ware, Tyson L., et al.
  Gepubliceerd in: (2019)